CN112300945A - Aspergillus niger solid-state fermentation feeding complex enzyme preparation and preparation process thereof - Google Patents
Aspergillus niger solid-state fermentation feeding complex enzyme preparation and preparation process thereof Download PDFInfo
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- CN112300945A CN112300945A CN202010548358.3A CN202010548358A CN112300945A CN 112300945 A CN112300945 A CN 112300945A CN 202010548358 A CN202010548358 A CN 202010548358A CN 112300945 A CN112300945 A CN 112300945A
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- aspergillus niger
- feed
- fermentation
- enzyme preparation
- solid
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- Enzymes And Modification Thereof (AREA)
Abstract
The invention relates to the technical field of fermentation engineering, in particular to a composite enzyme preparation for aspergillus niger solid-state fermentation feed production and a preparation process thereof. The aspergillus niger solid fermentation compound enzyme preparation for producing feed is prepared by solid fermentation of aspergillus niger strain QM-1, the preservation number of the strain is CGMCC No, 19629, the preservation date is 2020, 5 and 7 days, and the strain is preserved in the China general microbiological culture Collection center. The method solves the problems of low yield, high cost, complex fermentation process conditions and the like in the fermentation process; the feed complex enzyme preparation containing phytase, cellulase, pectinase, amylase, xylanase and beta-glucanase can be efficiently produced, the fermentation conditions are adjusted according to the proportion of the required feed enzyme preparation, the activity of certain enzyme is improved, the problems of low feed utilization rate and production efficiency in the production process of livestock are solved, the proper feed complex enzyme preparation is provided for the livestock at different growth stages, and the problem of contradiction between economic development and ecological protection of animal husbandry is solved.
Description
Technical Field
The invention relates to the technical field of fermentation engineering, in particular to a composite enzyme preparation for aspergillus niger solid-state fermentation feed production and a preparation process thereof.
Background
The complex enzyme for feed is a kind of bioactive high molecular substance which is synthesized in the organism and further collected, extracted and purified by manpower, acts in the animal body, has mild action condition, generally does not need strong acid and strong alkali, has high temperature and high pressure and low energy consumption, only needs to reduce activation energy and has no chemical pollution, and is a green natural biocatalyst. The exogenous enzyme is added into the livestock feed, so that the absorption of the animal to the nutrition in the feed can be promoted, the growth cycle can be shortened, the quality of meat products can be improved, the utilization rate of the feed can be improved, and the dependence of the livestock breeding industry on hormone can be reduced, therefore, the feed is widely applied to the livestock breeding industry.
The complex enzyme for feed has a plurality of enzyme systems which can catalyze and hydrolyze different substrates. The feed additive has positive effects on the problems that the digestive system of the ruminant larva is not developed and mature, corresponding enzymes are lacked in the digestive tract, the feed is not easy to digest and the like, and can effectively reduce the toxic action of antinutritional factors in the feed raw materials and supplement the deficiency of endogenous enzymes in livestock, thereby improving the digestibility and the utilization rate of the animal to the feed and improving the production performance of the animal breeding industry. Therefore, the addition of the complex enzyme for feed is an effective way for improving the digestibility of the feed. The enzymes contained in the complex enzyme preparation for feed mainly comprise phytase, cellulase, pectinase, amylase, xylanase, beta-glucanase and the like.
The phytase can decompose phytic acid to generate intermediate products such as inositol triphosphate and inositol monophosphate which can be used by livestock. If the animal body is lack of phytase, the phytic acid scaling on the inner wall of the alimentary canal can not be absorbed and utilized by the animal and is discharged out of the body in the form of feces, and phosphorus elements contained in the phytic acid are enriched in rivers through water circulation, so that the water body eutrophication and the like are caused.
The cellulase is a complex enzyme system, mainly comprises endoglucanase, exoglucanase, beta-glucosidase and the like, and has the following main functions: the viscosity of the feed in a livestock digestive system is reduced, and the metabolism and utilization of cellulose in the feed are accelerated; secondly, the feed has a protection function on gastric mucosa of the livestock and reduces the possibility of feed adhesion; thirdly, the cell wall of the fiber-containing substance in the feed is cracked, the dissolved substance is released, and the absorption rate is improved.
Pectinase is a generic term for a class of enzymes that can break down pectic substances and has various classifications. It has the main functions as follows: firstly, the bonding of the feed on the inner wall of the digestive tract is removed, and the production performance of animals is improved; ② the insufficiency of endogenous enzyme is supplemented, and the intestinal function is improved; and thirdly, the plant cell wall and the intercellular layer are disintegrated, and the feed conversion and utilization efficiency is improved. Animal cells cannot synthesize the enzyme per se, and the enzyme is necessary to be added into feed.
Amylases are a class of enzymes that specifically hydrolyze starch, and include mainly: alpha-amylase, beta-amylase, isoamylase and saccharifying enzyme. The main functions are as follows: the amylase in the immature animal is not secreted enough, and the amylase is added into the feed of the young animal, so that the adult period can be accelerated. ② the secretion and activity of endogenous digestive enzyme of animals are improved.
Xylanases include beta-1, 4-endoxylanase, beta-xylosidase, alpha-L-arabinosidase, alpha-D-glucuronidase, acetyl xylanase and phenolic acid esterase. The action in the feed is similar to that of the other enzymes mentioned above.
Beta-glucans are a class of homopolymers linked by d-glucoses with beta-2 glycosidic linkages, the most abundant in cereals. Most of livestock do not produce the enzymes in vivo, so that the beta-glucan in the grains can not be degraded, thereby reducing the digestibility of animals to the grains, and the addition of the beta-glucan in time can improve the daily gain of the livestock, the feed utilization rate and the nutrient digestibility and reduce the production cost.
The microbial solid fermentation feed enzyme is the most widely applied feed enzyme preparation production method at present, and the feed enzyme with rich varieties and high activity can be obtained. The natural world can produce a plurality of strains of the complex enzyme preparation for feed.
Aspergillus niger (Aspergillus niger), belonging to the kingdom of fungi, the phylum Anidiomycota, the subdivision Ascomycotina, the class Deuteromycetae, the order Hyphomycetales, the family Calycotinaceae, the genus Aspergillus, is a common strain of true silk, widely distributed in nature, and widely used in the fermentation industry, especially in the industries of feed enzyme preparations, vinegar brewing, fruit juice, sauce making and liquor making. The growth of the aspergillus niger has low requirements on nutrition and equipment, and the growth of the aspergillus niger can be satisfied as long as basic elements such as a water source, a nitrogen source, a carbon source and the like exist in a culture medium. A large number of researches show that Aspergillus niger solid fermentation can produce amylase, cellulase, pectinase, phytase, xylanase, beta-glucanase and the like, and can be used as animal feeding enzyme.
Aspergillus niger has strong growth and reproduction capability, simple and feasible culture conditions, difficult contamination by infectious microbes, high enzyme production speed, no harmful substances in a fermentation product, high yield and high secretion, is certified as a safe strain, and has wide commercial application in the fermentation industry. The bran is adopted for fermentation, so that the nutritional ingredients in the bran are fully utilized, the utilization value of the bran is improved, the raw materials are easy to obtain and low in price, the requirement on fermentation equipment is low, and the method is easy to popularize. In addition, Aspergillus niger is used as a host bacterium, has strong secretion and modification capability and post-translational processing capability similar to that of mammals, and the genetic stability of a recombinant is good, so the Aspergillus niger has a plurality of high-activity enzyme expression systems.
Aspergillus niger fermentation has liquid fermentation, solid fermentation and other fermentation modes, but the solid fermentation medium is easy to prepare, the culture and fermentation process is simple, and the fermentation cost is low. The utilization of Aspergillus niger solid fermentation to produce complex enzyme preparation for feed is a hot spot of research in recent years. The feed enzyme can improve the utilization rate of various nutrient metabolism in daily ration of livestock, reduce daily dosage, promote the production of livestock, and the enzyme preparation is bioactive molecule, and can be decomposed in livestock without accumulation in vivo to affect meat quality, and the enzyme preparation can also improve the stress ability and immunity of livestock and reduce the content of nitrogen and phosphorus in excrement. The livestock husbandry of the Qinghai-Tibet plateau is developed, cattle, sheep and poultry cultivation bases are numerous, the required feed amount is huge, the grassland is degraded due to the large grazing amount, the water eutrophication can be caused due to the excessive nitrogen and phosphorus in the animal excrement, and the ecological environment of the area is threatened.
At present, when bran is used as a fermentation medium in aspergillus niger solid fermentation, rich complex enzyme for feed can be fermented, but factors such as carbon source-nitrogen source ratio, additional nitrogen source types, temperature, pH and the like of the medium have different influences on enzyme production activity.
Disclosure of Invention
Based on the problems, the invention aims to provide a compound enzyme preparation for aspergillus niger solid-state fermentation and feed production and a preparation process thereof.
An Aspergillus niger solid state fermentation feeding complex enzyme preparation, wherein the Aspergillus niger solid state fermentation feeding complex enzyme preparation is prepared by solid state fermentation of Aspergillus niger strain QM-1, the preservation number of the Aspergillus niger strain QM-1 is CGMCC No, 19629, the preservation date is 2020, 5, 7 and is preserved in China general microbiological culture Collection center (CGMCC for short, with the address of No. 3 Hosth No. 1 of the North Chen West Lu of the Yangyang area of Beijing); the complex enzyme preparation for feed comprises 6 kinds of complex enzymes for feed: phytase, cellulase, pectinase, amylase, xylanase and beta-glucanase.
The preparation process of the composite enzyme preparation for aspergillus niger solid-state fermentation and feed production comprises the following specific steps:
s1, obtaining the high-yield compound enzyme strain: inoculating common Aspergillus niger strains under laboratory conditions to a PDA culture medium, respectively irradiating with ultraviolet rays with the amplitude of more than or equal to 300Lx for 30s, 60s, 90s and 120s, repeatedly screening at the culture temperature of 30 ℃, performing enzyme activity determination, and screening out Aspergillus niger strains QM-1 with high enzyme activity and high enzyme quantity for producing feeding enzymes through multiple rounds of ultraviolet mutagenesis;
s2, inoculating and activating aspergillus niger strain QM-1: preparing a slant activation culture medium, inoculating aspergillus niger strain QM-1 for strain activation, and culturing for 72h in a constant-temperature incubator at 30 ℃;
s3, solid fermentation culture: the method comprises the following steps of: the soybean meal is used as a carbon source and a nitrogen source in a ratio of 3-15: 0-5, ammonium sulfate, ammonium nitrate, sodium nitrate, beef extract or yeast extract is used as an additional nitrogen source, and a solid fermentation culture medium is prepared according to a material-distilled water ratio of 10: 8; inoculating S2 activated aspergillus niger strain QM-1, and fermenting for 5-6 days at the temperature of 25-30 ℃ and the pH of 3.0-8.0 to obtain a feed complex enzyme preparation containing 6 feed complex enzymes;
s4, enzyme activity assay: the phytase activity determination method adopts a ferrous sulfate-ammonium molybdate method; the enzyme activities of the cellulase, the pectinase, the amylase, the beta-glucanase and the xylanase adopt a DNS method. Wherein, the quality of the enzyme preparation is evaluated by the activity, purity, stability, formula and package, and finally the quality of the product is identified to ensure the safety and high activity of the product.
Further, the PDA culture medium in S1 is potato glucose agar culture medium, wherein potato 200g, glucose 20g, agar 20g, distilled water 1000mL natural pH.
Further, the slant activation medium in S2 is potato dextrose agar medium, wherein potato 200g, dextrose 20g, agar 20g, distilled water 1000mL, natural pH.
Further, the optimized ratio of the bran to the soybean meal in the S3 is 10:0, 9:1, 8:2, 7:3 and 6: 4.
Further, the solid fermentation culture conditions of the 6 feeding compound enzymes with higher activity are as follows: fermentation temperature 30 ℃, bran: the soybean meal is 7:3, ammonium nitrate is used as an additional nitrogen source, the pH value is 7, and the fermentation time is 6 days.
Compared with the prior art, the invention has the following beneficial effects: the method solves the problems of low yield, high cost, complex fermentation process conditions and the like in the fermentation process. The technology can efficiently produce the feed complex enzyme preparation containing phytase, cellulase, pectinase, amylase, xylanase and beta-glucanase, adjust the fermentation conditions according to the proportion of the required feed enzyme preparation, improve the activity of a certain enzyme, solve the problems of low feed utilization rate and low production efficiency in the production process of livestock, provide proper feed complex enzyme preparation for livestock in different growth stages, and solve the problem of contradiction between economic development and ecological protection of animal husbandry.
Drawings
FIG. 1 is a diagram of Aspergillus niger QM1 strain according to the present invention;
FIG. 2 shows a complex enzyme preparation for feed obtained by solid fermentation of the strain QM1 Aspergillus niger of the present invention;
FIG. 3 shows the green feed for grass block, grass particle and grass powder prepared by the complex enzyme preparation for feed.
Detailed Description
The technical solutions of the present invention will be described clearly and completely with reference to the following embodiments, and it should be understood that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
Example 1
An Aspergillus niger solid state fermentation feeding complex enzyme preparation, wherein the Aspergillus niger solid state fermentation feeding complex enzyme preparation is prepared by solid state fermentation of Aspergillus niger strain QM-1, the preservation number of the Aspergillus niger strain QM-1 is CGMCC No, 19629, the preservation date is 2020, 5, 7 and is preserved in China general microbiological culture Collection center (CGMCC for short, with the address of No. 3 Hosth No. 1 of the North Chen West Lu of the Yangyang area of Beijing); the complex enzyme preparation for feed comprises 6 kinds of complex enzymes for feed: phytase, cellulase, pectinase, amylase, xylanase and beta-glucanase.
The preparation process of the composite enzyme preparation for aspergillus niger solid-state fermentation and feed production comprises the following specific steps:
(1) obtaining of high-yield complex enzyme strain
Inoculating common Aspergillus niger strains under laboratory conditions to a PDA culture medium, respectively irradiating with ultraviolet rays with amplitude of more than or equal to 300Lx for 30s, 60s, 90s and 120s, repeatedly screening at the culture temperature of 30 ℃, performing enzyme activity determination, and screening out Aspergillus niger strains QM-1 (detailed in figure 1) with high enzyme activity and high enzyme yield for producing feeding enzymes through multiple rounds of ultraviolet mutagenesis; wherein, the PDA culture medium is 200g of potato, 20g of glucose, 20g of agar and 1000mL of distilled water with natural pH.
(2) Aspergillus niger strain QM-1 inoculation activation
Preparing a slant activation culture medium, wherein 200g of potatoes, 20g of glucose, 20g of agar and 1000mL of distilled water have natural pH, inoculating aspergillus niger strain QM-1 to activate strains, and culturing for 72 hours in a constant-temperature incubator at 30 ℃;
(3) solid fermentation culture step
1) Optimization of solid fermentation culture conditions-single factor experiment
Through single factor experiment, comparing the enzyme activities under different conditions, selecting the optimum conditions.
The results show that the respective enzyme activities were relatively high at pH 5; when the fermented feed is fermented at the temperature of 30 ℃, the activity of various enzymes is relatively high, the temperature of the fermented feed is close to the body temperature of animals at the temperature of 30 ℃, and the enzyme preparation has obvious effect when being put into the feed; at 60 ℃, the enzyme activities of the four enzymes are at a relatively high value; when the fermentation days are 5 days, the activity of each enzyme is relatively high.
Through multiple experiments, the single-factor experiment result is determined, and the aspergillus niger strain QM-1 solid fermentation process flow is as follows: the optimal culture medium proportion is that bean pulp: bran 4: 6, the optimal material distilled water ratio is 10:8, the optimal fermentation temperature is 30 ℃, the optimal pH value is 4.6, and the optimal fermentation culture time is 144 h. Under the condition, the measured cellulase activity is 3089U/g, pectinase 558U/g, amylase 508U/g, beta-glucanase 55U/g, phytase 943U/g and xylanase 651U/g.
2) Solid fermentation culture condition optimization-orthogonal experiment
Due to the interaction among different factors, orthogonal experiments are carried out on the QM-1 strain for solid fermentation feeding complex enzyme preparation under different conditions.
On the basis of the previous test, the orthogonal test is determined to be a four-factor three-level (see table 1 in detail), and an orthogonal table L is selected9(34) Design (see table 2 for details).
TABLE 1 orthogonal test factor horizon
TABLE 2L9(34) Orthogonal table
TABLE 3 enzyme activities under orthogonal test
The results of the orthogonal experiments show that: bran at 30 ℃, bran: the highest phytase activity of 370.00(U/mL) produced by culturing Aspergillus niger when the soybean meal is 8:2, ammonium nitrate is an additional nitrogen source and the pH value is 7; bran at 28 ℃, bran: culturing Aspergillus niger under the conditions of soybean meal of 8:2, sodium nitrate and pH of 8 to produce cellulase by fermentation, wherein the enzyme activity is 506.43(U/mL) which is the highest; culturing Aspergillus niger to produce pectinase under the conditions of 28 deg.C, bran, soybean meal (7: 3), ammonium nitrate and pH (6), wherein the enzyme activity is 719.30(U/mL) to the maximum; bran at 28 ℃, bran: bean pulp is 6:4, beef extract is used as a nitrogen source, pH is 7, amylase is produced after 6 days of culture as the optimal culture condition, and the enzyme activity is 2872 (U/mL); bran at 25 ℃, bran: the xylanase activity produced by culturing aspergillus niger under the conditions that the soybean meal is 7:3, sodium nitrate is selected as an additional nitrogen source and the pH value is 7 is the highest at 507.05 (U/mL); bran at 25 ℃, bran: the highest activity of beta-glucanase produced by aspergillus niger is 2501(U/mL) when the soybean meal is 8:2 and the beef extract is used as an additional nitrogen source and the pH value is 6.
3) Solid fermentation culture
The optimal process conditions for producing 6 feed enzymes by the solid fermentation of the aspergillus niger strain QM-1 are different, and the fermentation process conditions can be selected in a targeted manner when the feed complex enzyme is produced, so that a complex enzyme preparation for efficiently producing a certain enzyme is obtained; or the 6 feeding compound enzymes can be selected to have higher activity. Namely, the method comprises the following steps of: preparing a solid fermentation culture medium by using bean pulp as a carbon source and a nitrogen source in a ratio of 7:3, using ammonium nitrate as an additional nitrogen source and using distilled water in a ratio of 10: 8; inoculating S2 activated Aspergillus niger strain QM-1, and fermenting at 30 deg.C and pH 7.0 for 6 days to obtain complex enzyme preparation for feed containing 6 kinds of complex enzymes (see figure 2).
Determining the enzyme activity of the phytase to be 211(U/mL) by adopting a ferrous sulfate-ammonium molybdate method; the activity of the cellulase is 441(U/mL), the activity of the pectinase is 719 (U/mL), the activity of the amylase is 2467(U/mL), the activity of the xylanase is 365(U/mL) and the activity of the beta-glucanase is 2223(U/mL) which are determined by a DNS method.
Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that changes, modifications, substitutions and alterations can be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.
Claims (6)
1. The compound enzyme preparation for aspergillus niger solid state fermentation and feed production is characterized by being prepared by solid state fermentation of aspergillus niger strain QM-1, wherein the preservation number of the aspergillus niger strain QM-1 is CGMCC No, 19629, the preservation date is 2020, 5, 7 days, and the compound enzyme preparation is preserved in the China general microbiological culture Collection center; the complex enzyme preparation for feed comprises 6 kinds of complex enzymes for feed: phytase, cellulase, pectinase, amylase, xylanase and beta-glucanase.
2. A preparation process of a composite enzyme preparation for aspergillus niger solid-state fermentation and feed production is characterized by comprising the following specific steps:
s1, obtaining the high-yield compound enzyme strain: inoculating common Aspergillus niger strains under laboratory conditions to a PDA culture medium, respectively irradiating with ultraviolet rays with the amplitude of more than or equal to 300Lx for 30s, 60s, 90s and 120s, repeatedly screening at the culture temperature of 30 ℃, performing enzyme activity determination, and screening out Aspergillus niger strains QM-1 with high enzyme activity and high enzyme quantity for producing feeding enzymes through multiple rounds of ultraviolet mutagenesis;
s2, inoculating and activating aspergillus niger strain QM-1: preparing a slant activation culture medium, inoculating aspergillus niger strain QM-1 for strain activation, and culturing for 72h in a constant-temperature incubator at 30 ℃;
s3, solid fermentation culture: the method comprises the following steps of: the soybean meal is used as a carbon source and a nitrogen source in a ratio of 3-15: 0-5, ammonium sulfate, ammonium nitrate, sodium nitrate, beef extract or yeast extract is used as an additional nitrogen source, and a solid fermentation culture medium is prepared according to a material-distilled water ratio of 10: 8; inoculating S2 activated aspergillus niger strain QM-1, and fermenting for 5-6 days at the temperature of 25-30 ℃ and the pH of 3.0-8.0 to obtain a feed complex enzyme preparation containing 6 feed complex enzymes;
s4, enzyme activity assay: the phytase activity determination method adopts a ferrous sulfate-ammonium molybdate method; the enzyme activities of the cellulase, the pectinase, the amylase, the beta-glucanase and the xylanase adopt a DNS method.
3. The preparation process of the aspergillus niger solid-state fermentation composite enzyme preparation for feed production according to claim 2, wherein the PDA medium in S1 is a potato dextrose agar medium, wherein 200g of potato, 20g of glucose, 20g of agar, 1000mL of distilled water has a natural pH.
4. The preparation process of the aspergillus niger solid-state fermentation composite enzyme preparation for feed production according to claim 2, wherein the slant activation medium in S2 is a potato dextrose agar medium, wherein 200g of potato, 20g of glucose, 20g of agar, 1000mL of distilled water, and natural pH.
5. The preparation process of the aspergillus niger solid-state fermentation composite enzyme preparation for feed production according to claim 2, wherein the optimized ratio of the bran to the soybean meal of S3 is 10:0, 9:1, 8:2, 7:3, 6: 4.
6. The preparation process of the aspergillus niger solid-state fermentation composite enzyme preparation for feed production according to claim 2, wherein the 6 kinds of composite enzyme preparation for feed with higher activity are cultured under the solid fermentation conditions that: fermentation temperature 25 ℃, bran: the soybean meal is 7:3, ammonium nitrate is used as an additional nitrogen source, the pH value is 7, and the fermentation time is 6 days.
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